147613-78-3Relevant articles and documents
Synthesis and electrochemical behaviour of [60]fullerene possessing poly(arylacetylene) dendrimer addends
Avent, Anthony G.,Birkett, Paul R.,Paolucci, Francesco,Roffia, Sergio,Taylor, Roger,Wachter, Norbert K.
, p. 1409 - 1414 (2007/10/03)
61,61-Bis[4-{3,5-bis(3,5-di-tert-butylphenylethynyl)phenylethynyl}phenyl ]-1,2-dihydro-1,2-methano[60]fullerene (10) and 61,61-bis[4-{3,5-bis[3,5-bis(3,5-di-tert-butylphenylethynyl)phenylethynyl]phenyl ethynyl}phenyl]-1,2-dihydro-1,2-methano[60]fullerene
The 'Inverse Electron-demand' Diels-Ader Reaction in Polymer Synthesis. Part 1. A Convenient Synthetic Route to Diethynyl Aromatic Compounds
Royles, Brodyck J. L.,Smith, David M.
, p. 355 - 358 (2007/10/02)
The simple procedure whereby acetophenone derivatives are converted, by reaction with phosphoryl chloride and N,N-dimethylformamide, into β-chlorocinnamaldehydes, and thence, by base-induced elimination, into ethynylarenes, has been extended to diketones of the type MeCOC6H4COMe (m- and p-) and (p-MeCOC6H4)2X (X = O, S, SO2, CH2, CO, or a single bond): the corresponding diethynyl compounds are obtained by this route in acceptable yield. 1,3,5-Triacetylbenzene is similarly converted into 1,3,5-triethynylbenzene.